| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65720478-65720593 | Common:1; Rare:68 | ||||
| chr11:65856951-65857329 | Common:4; Rare:113 | ||||
| chr11:65860356-65860466 | Common:1; Rare:34 | ||||
| chr11:65872730-65872938 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65879703-65879847 | Common:2; Rare:35 | ||||
| chr11:65888425-65888682 | Common:1; Rare:90 | ||||
| chr11:65890457-65890674 | Common:3; Rare:67 | ||||
| chr11:65900386-65900456 | Common:1; Rare:12 | ||||
| chr11:65961617-65961758 | Rare:43 | ||||
| chr11:66002102-66002304 | Common:1; Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:66002458-66002543 | Rare:23; Clinvar:1 | ||||
| chr11:66021135-66021230 | Rare:28 | ||||
| chr11:66058058-66058405 | Rare:87 | ||||
| chr11:66070848-66070974 | Rare:30 | ||||
| chr11:66257602-66257864 | Common:1; Rare:75 |